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出芽酵母分离酶Esp1在Ty1元件逆转录转座中的作用。

A role for the budding yeast separase, Esp1, in Ty1 element retrotransposition.

作者信息

Ho Krystina L, Ma Lina, Cheung Stephanie, Manhas Savrina, Fang Nancy, Wang Kaiqian, Young Barry, Loewen Christopher, Mayor Thibault, Measday Vivien

机构信息

Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, British Columbia, Canada; Wine Research Centre, University of British Columbia, Vancouver, British Columbia, Canada.

Wine Research Centre, University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

PLoS Genet. 2015 Mar 30;11(3):e1005109. doi: 10.1371/journal.pgen.1005109. eCollection 2015 Mar.

DOI:10.1371/journal.pgen.1005109
PMID:25822502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4378997/
Abstract

Separase/Esp1 is a protease required at the onset of anaphase to cleave cohesin and thereby enable sister chromatid separation. Esp1 also promotes release of the Cdc14 phosphatase from the nucleolus to enable mitotic exit. To uncover other potential roles for separase, we performed two complementary genome-wide genetic interaction screens with a strain carrying the budding yeast esp1-1 separase mutation. We identified 161 genes that when mutated aggravate esp1-1 growth and 44 genes that upon increased dosage are detrimental to esp1-1 viability. In addition to the expected cell cycle and sister chromatid segregation genes that were identified, 24% of the genes identified in the esp1-1 genetic screens have a role in Ty1 element retrotransposition. Retrotransposons, like retroviruses, replicate through reverse transcription of an mRNA intermediate and the resultant cDNA product is integrated into the genome by a conserved transposon or retrovirus encoded integrase protein. We purified Esp1 from yeast and identified an interaction between Esp1 and Ty1 integrase using mass spectrometry that was subsequently confirmed by co-immunoprecipitation analysis. Ty1 transposon mobility and insertion upstream of the SUF16 tRNA gene are both reduced in an esp1-1 strain but increased in cohesin mutant strains. Securin/Pds1, which is required for efficient localization of Esp1 to the nucleus, is also required for efficient Ty1 transposition. We propose that Esp1 serves two roles to mediate Ty1 transposition - one to remove cohesin and the second to target Ty1-IN to chromatin.

摘要

分离酶/Esp1是一种蛋白酶,在后期开始时发挥作用,切割黏连蛋白,从而使姐妹染色单体分离。Esp1还能促进Cdc14磷酸酶从核仁中释放出来,从而实现有丝分裂退出。为了揭示分离酶的其他潜在作用,我们用携带芽殖酵母esp1-1分离酶突变的菌株进行了两项互补的全基因组遗传相互作用筛选。我们鉴定出161个基因,这些基因发生突变时会加剧esp1-1的生长缺陷,还有44个基因,剂量增加时对esp1-1的生存能力有害。除了鉴定出预期的细胞周期和姐妹染色单体分离基因外,在esp1-1遗传筛选中鉴定出的基因中有24%在Ty1元件逆转录转座中起作用。逆转座子与逆转录病毒一样,通过mRNA中间体的逆转录进行复制,产生的cDNA产物由保守的转座子或逆转录病毒编码的整合酶蛋白整合到基因组中。我们从酵母中纯化了Esp1,并通过质谱鉴定了Esp1与Ty1整合酶之间的相互作用,随后通过免疫共沉淀分析得到证实。在esp1-1菌株中,Ty1转座子的移动性和在SUF16 tRNA基因上游的插入均降低,但在黏连蛋白突变菌株中增加。Securin/Pds1是Esp1有效定位到细胞核所必需的,也是有效进行Ty1转座所必需的。我们提出,Esp1在介导Ty1转座中发挥两个作用——一个是去除黏连蛋白,另一个是将Ty1-IN靶向染色质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/c9e052466ec8/pgen.1005109.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/a5ed2089eaa5/pgen.1005109.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/aa249468f970/pgen.1005109.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/fa186db16199/pgen.1005109.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/8fc41a050142/pgen.1005109.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/2f5de9511187/pgen.1005109.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/da6410847dd5/pgen.1005109.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/a91665c43d0e/pgen.1005109.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/ba79dc0e50f9/pgen.1005109.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/a7ba709b3f26/pgen.1005109.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/c9e052466ec8/pgen.1005109.g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/a5ed2089eaa5/pgen.1005109.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/aa249468f970/pgen.1005109.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/fa186db16199/pgen.1005109.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/8fc41a050142/pgen.1005109.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/2f5de9511187/pgen.1005109.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/da6410847dd5/pgen.1005109.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/a91665c43d0e/pgen.1005109.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/ba79dc0e50f9/pgen.1005109.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/a7ba709b3f26/pgen.1005109.g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/374b/4378997/c9e052466ec8/pgen.1005109.g010.jpg

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Science. 2014 Nov 21;346(6212):963-7. doi: 10.1126/science.1256917.
2
Dyskerin, tRNA genes, and condensin tether pericentric chromatin to the spindle axis in mitosis.在有丝分裂过程中,戴斯科林、转运RNA基因和凝聚素将着丝粒周围染色质连接到纺锤体轴上。
J Cell Biol. 2014 Oct 27;207(2):189-99. doi: 10.1083/jcb.201405028. Epub 2014 Oct 20.
3
The Scc2-Scc4 complex acts in sister chromatid cohesion and transcriptional regulation by maintaining nucleosome-free regions.
酵母 Ty 反转录转座子家族整合位点选择机制中的光与影。
Curr Genet. 2021 Jun;67(3):347-357. doi: 10.1007/s00294-021-01154-7. Epub 2021 Feb 15.
4
Structure and Function of the Separase-Securin Complex.分离酶-抑制蛋白复合物的结构与功能。
Subcell Biochem. 2021;96:217-232. doi: 10.1007/978-3-030-58971-4_4.
5
PP2A dephosphorylates Pds1 and inhibits spindle elongation in .PP2A 去磷酸化 Pds1 并抑制. 的纺锤体伸长。
J Cell Sci. 2020 Jul 29;133(14):jcs243766. doi: 10.1242/jcs.243766.
6
Evolutionary repair: Changes in multiple functional modules allow meiotic cohesin to support mitosis.进化修复:多个功能模块的改变使减数分裂黏连蛋白能够支持有丝分裂。
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7
Retrotransposon targeting to RNA polymerase III-transcribed genes.逆转录转座子靶向RNA聚合酶III转录的基因。
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8
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10
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Genome Res. 2012 Apr;22(4):704-13. doi: 10.1101/gr.129585.111. Epub 2012 Jan 4.